Matches in SemOpenAlex for { <https://semopenalex.org/work/W4328049338> ?p ?o ?g. }
- W4328049338 abstract "Synthetic methodology is considered a holy grail in both organic chemistry and materials science. Over the past few decades, researchers have explored graphene-type molecules (or nanographenes) through classic Scholl oxidative cyclodehydrogenation. Despite the successes achieved with various nanographenes, the development of new methods to synthesize these highly desired molecules lags behind. Herein, we developed a facile and effective method to produce a series of nanographenes bearing nitrogen (N)-doped pentagon-heptagon pairs in acceptable yields. Modification of the heptagonal ring endowed the resultant nanographenes with tunable physicochemical properties; for instance, M9 exhibited both aggregation-caused quenching and aggregation-induced emission behavior. Most strikingly, novel nanographenes containing N-doped pentagon-octagon pairs were also obtained using the same synthetic strategy, demonstrating the superior versatility and efficiency of the proposed ring expansion method." @default.
- W4328049338 created "2023-03-22" @default.
- W4328049338 creator A5080624986 @default.
- W4328049338 creator A5090537271 @default.
- W4328049338 date "2023-04-17" @default.
- W4328049338 modified "2023-10-18" @default.
- W4328049338 title "Facile Synthesis of Nitrogen‐Doped Nanographenes with Joined Nonhexagons via a Ring Expansion Strategy" @default.
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- W4328049338 doi "https://doi.org/10.1002/anie.202302761" @default.
- W4328049338 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36942506" @default.
- W4328049338 hasPublicationYear "2023" @default.
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- W4328049338 hasAuthorship W4328049338A5080624986 @default.
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